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Anchorage

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
ANCHORAGE FDA UDI
Generic Name
Surgical instrument/implant rack FDA UDI
Device Name
Screw Rack Lid CP FDA UDI
Model / Reference
940471 FDA UDI
Description
Screw Rack Lid CP FDA UDI

Identifiers

Catalog Number
940471 FDA UDI
Primary DI / UDI-DI
07613327277531 FDA UDI
FDA Product Code
HRS FDA UDI
HWC FDA UDI
GMDN Term
Surgical instrument/implant rack FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument/implant rack

Anchorage by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument/implant rack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 6017bde8-6993-411d-9ab0-99387a2514c1 34 fields · synced May 30, 2026